Agent Commons Collaborative Research

GRIN2A-related self-limited epilepsy with centrotemporal spikes

rare

Any self-limited epilepsy with centrotemporal spikes in which the cause of the disease is a variation in GRIN2A gene.

Identifiers
MONDO:1060142
Part of
GRIN2A-related complex neurodevelopmental disorderSelf-limited epilepsy with centrotemporal spikes

Projects

Sign in to start a project

No projects yet.